首页> 外文期刊>Analytical and quantitative cytology and histology >Improved correction of quantitative nuclear DNA (ploidy) measurements in tissue sections.
【24h】

Improved correction of quantitative nuclear DNA (ploidy) measurements in tissue sections.

机译:改进了组织切片中定量核DNA(倍性)测量的校正。

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

OBJECTIVE: To evaluate, using a computer model, the advantages for ploidy measurements of selecting only center-containing sections of nuclei in ultrathin, very thick or relatively thick tissue sections. STUDY DESIGN: The computed corpuscle sectioning program was run on a personal computer. Its synthetic data were corrected by a variety of correction algorithms. RESULTS: When only center-containing sections of nuclei were selected in ultrathin sections, spherical nuclei could be corrected perfectly, and mildly prolate ellipsoidal nuclei with a selection bias in favor of elliptical nuclear section profiles could be corrected with high fidelity. Ultrathin sections most faithfully represented the true height of the peak of highest ploidy and showed better peak discrimination than other choices of section thickness, but small sample size, wavy sections, markedly inhomogeneous intranuclear DNA distribution and oblate ellipsoidal nuclei represented significant limitations of this approach. As nuclear prolation increased, peak definition worsened, and the peak of highest ploidy was falsely shortened. Results were unaffected by errors in the estimation of section thickness when an internal diploid standard was used. The effect of variable internuclear DNA concentration in mildly or moderately prolate ellipsoidal nuclei was nil. The choice of correction algorithm was unimportant, except that the reference curve method was better able to analyze oblate ellipsoidal nuclei, wavy sections and nuclei with inhomogeneous intranuclear DNA, and provided superior insight into nuclear and section parameters. Thick and very thick sections did not require correction and, unlike ultrathin sections, were immune to markedly inhomogeneous intranuclear DNA distribution, to nonspherical nuclear shape and to focal variation in section thickness (waviness), but (in relatively thick more than in very thick sections) the height of the peak of highest ploidy was falsely shortened, often markedly, and peak definition was worse. CONCLUSION: Choice of section thickness and selection of only center-containing nuclear sections for analysis with a bias in favor of elliptical nuclear section profiles in ultrathin sections are very important for optimal results; the choice of correction algorithm is less important.
机译:目的:使用计算机模型评估倍性测量的优势,即仅选择超薄,非常厚或相对较厚的组织切片中包含核的中心切片。研究设计:计算的小体切片程序在个人计算机上运行。其综合数据已通过多种校正算法进行了校正。结果:在超薄切片中仅选择核的含中心部分时,球形核可以得到完美矫正,对椭圆形核截面轮廓有利的具有选择偏见的轻度长椭圆形核可以被高保真度校正。超薄切片最能忠实地代表最高倍性峰的真实高度,并且显示出比其他切片厚度选择更好的峰辨别力,但是小样本量,波浪形切片,明显的核内DNA分布不均和椭圆形椭圆形核代表了该方法的显着局限性。随着核比例增加,峰的清晰度变差,最高倍性峰被错误地缩短。当使用内部二倍体标准品时,结果不受断面厚度估计误差的影响。轻度或中度长椭圆形核中可变核内DNA浓度的影响为零。校正算法的选择并不重要,除了参考曲线方法能够更好地分析扁圆形的椭圆形核,波浪形截面和具有不均匀核内DNA的核,并提供对核和截面参数的深入了解。厚和非常厚的部分不需要校正,并且与超薄部分不同,它们对明显不均匀的核内DNA分布,非球形核形状和部分厚度(波纹度)的局部变化具有免疫力,但是(相对厚于非常厚的部分) )最高倍性峰的高度被错误地缩短了,通常明显地缩短了,峰的清晰度也变差了。结论:为了获得最佳结果,选择截面厚度和选择仅用于分析的中心含核截面(偏向于椭圆形截面的超薄截面)对分析至关重要。校正算法的选择不太重要。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号